Liu Wang-Jing, Shiung Hui-Jui, Lo Chu-Fang, Leu Jiann-Horng, Lai Ying-Jang, Lee Tai-Lin, Huang Wei-Tung, Kou Guang-Hsiung, Chang Yun-Shiang
Department of Earth and Life Science, University of Taipei, Taipei, Taiwan.
Department of Molecular Biotechnology, Da-Yeh University, Changhua, Taiwan.
PLoS One. 2014 Jan 21;9(1):e85779. doi: 10.1371/journal.pone.0085779. eCollection 2014.
White spot syndrome virus (WSSV) is a large enveloped virus. The WSSV viral particle consists of three structural layers that surround its core DNA: an outer envelope, a tegument and a nucleocapsid. Here we characterize the WSSV structural protein VP11 (WSSV394, GenBank accession number AF440570), and use an interactome approach to analyze the possible associations between this protein and an array of other WSSV and host proteins. Temporal transcription analysis showed that vp11 is an early gene. Western blot hybridization of the intact viral particles and fractionation of the viral components, and immunoelectron microscopy showed that VP11 is an envelope protein. Membrane topology software predicted VP11 to be a type of transmembrane protein with a highly hydrophobic transmembrane domain at its N-terminal. Based on an immunofluorescence assay performed on VP11-transfected Sf9 cells and a trypsin digestion analysis of the virion, we conclude that, contrary to topology software prediction, the C-terminal of this protein is in fact inside the virion. Yeast two-hybrid screening combined with co-immunoprecipitation assays found that VP11 directly interacted with at least 12 other WSSV structural proteins as well as itself. An oligomerization assay further showed that VP11 could form dimers. VP11 is also the first reported WSSV structural protein to interact with the major nucleocapsid protein VP664.
白斑综合征病毒(WSSV)是一种大型包膜病毒。WSSV病毒粒子由围绕其核心DNA的三层结构组成:外层包膜、皮层和核衣壳。在此,我们对WSSV结构蛋白VP11(WSSV394,GenBank登录号AF440570)进行了表征,并采用相互作用组学方法分析该蛋白与一系列其他WSSV和宿主蛋白之间可能存在的关联。时间转录分析表明vp11是一个早期基因。对完整病毒粒子进行蛋白质免疫印迹杂交及病毒成分分级分离,以及免疫电子显微镜观察显示VP11是一种包膜蛋白。膜拓扑结构软件预测VP11是一种跨膜蛋白,其N端有一个高度疏水的跨膜结构域。基于对转染VP11的Sf9细胞进行的免疫荧光测定以及对病毒粒子的胰蛋白酶消化分析,我们得出结论,与拓扑结构软件的预测相反,该蛋白的C端实际上位于病毒粒子内部。酵母双杂交筛选结合免疫共沉淀试验发现,VP11与至少12种其他WSSV结构蛋白以及其自身直接相互作用。寡聚化试验进一步表明VP11可以形成二聚体。VP11也是首个被报道与主要核衣壳蛋白VP664相互作用的WSSV结构蛋白。